Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 85630

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
December 19, 2017
Product types
Device
Classifications
Class III
Statuses
Terminated
Recalling firm wording
PerkinElmer Health Sciences, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

PerkinElmer 226 Sample Collection Device

Z-2264-2020
Recall number
Z-2264-2020
Initiated
December 19, 2017
Classification
Class III
Status
Terminated
Quantity
164,952 devices

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
PerkinElmer 226 Sample Collection Devices Lot Number 40020001 had serial numbers printed on the pack labels that did not match the serial number range of the devices contained within the pack.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

PerkinElmer 226 Sample Collection Devices Lot Number 40020001 had serial numbers printed on the pack labels that did not match the serial number range of the devices contained within the pack.

Code information

UDI: (01)50812589020011(17)200831(10)40020001; Serial Numbers: 06879601-06879700

Distribution pattern

US distribution in the state of Ohio